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abiotrophy
adult polyglucosan body disease
advances in neurology
algorithm
Alzheimer's disease
aminoacidopathies
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, bulbar
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, childhood
amyotrophic lateral sclerosis, conjugal
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
amyotrophic lateral sclerosis, juvenile
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis, Parkinson-dementia-complex
amyotrophic lateral sclerosis, post-encephalitic
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
anterior horn cell disease
aphasia
aphasia, progressive, primary
areflexia
arm weakness
arthrogryposis multiplex
ataxia
ataxia, progressive
autonomic dysfunction
axonal degeneration
Babinski sign
behavioral disorder
bladder dysfunction
brain atrophy
bulbar palsy
bulbar palsy, childhood
bulbar palsy, progressive
C0ORF72
CAG repeats
calf hypertrophy
camptocormia
cane
CAT scan, abnormal
CAT scan, emission, abnormal
cataracts
central core disease
cerebellar atrophy, primary
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, cell count
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, protein of
cerebrovascular accident
Charcot-Marie-Tooth
children
chorea
chromosomal abnormality
chromosome 5
cognition
congenital heart disease
crying, pathologic
deafness
degenerative diseases of CNS
Dejerine-Sottas syndrome
delusion
dementia
dementia, age at onset
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dermatomyositis
developmental retardation
diagnostic criteria
differential diagnosis
difficulty climbing stairs
distal muscle atrophy
distal muscle weakness
DNA probes
drooling
dying
dysarthria
dysphagia
dyspnea
dystonia
electromyogram
emotional lability
epidemiology of neurology
episodic neurologic deficits
exercise
exercise intolerance
facial weakness
facial weakness, bilateral
falling
familial
fasciculation
Fazio-Londe's disease
fibrillations
floppy infant
fluency
foot drop
free radical
Friedreich's ataxia
frontal lobe, atrophy
frontotemporal dementia, behavioral variant
gait disorder
gait, spastic
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glycogen storage disease
Guillain Barre syndrome
gynecomastia
hallucination
hand weakness
hearing loss
heavy metal intoxication
hemiparesis
heralding manifestation
history of neurology
hoarseness
Huntington's chorea
hyperpigmentation of skin
hyperreflexia
hyporeflexia
hypotension, systemic
hypotonia
hypotonia, infants
imbalance
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
incontinentia pigmenti
infant, evaluation of
inflexibility, mental
intellectual deficit
intellectual deterioration
intrinsic hand muscles, wasting of
Isaacs syndrome
Jakob-Creutzfeldt disease
jaw jerk, abnormal
Jewish
klippel feil syndrome
Kugelberg-Welander syndrome
lactic acidemia
lathyrism
laughing
laughing, pathologic
leg atrophy
leg weakness, bilateral
leg weakness, unilateral
leukodystrophy
leukoencephalopathy
Lewy body
life expectancy
lobar atrophy
lysosomal storage disease
malformation, CNS, congenital
memory, defect of recent
memory, impairment of
mental retardation
metabolic disorder, primary
Mills syndrome
mimics
misdiagnosis
molecular genetics
monomelic amyotrophy
mononeuropathy
mortality
motor neuron disease
MRI, abnormal
multiple sclerosis, differential diagnosis of
muscle atrophy, progressive
muscle cramp
muscle diseases, characteristics of
muscle hypertrophy
muscle twitching
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenic crisis
myelomalacia
myeloneuropathy
myokymia
myopathy
myopathy, carcinomatous
myopathy, thyroid disease causing
myositis
myotonia dystrophica
nasal speech
neck weakness
nerve conduction studies
neuritis, causes of
neuroendocrinology
neurofibrillary degeneration
neurofibromatosis 1
neurofibromatosis 2
neurogenic bladder
neurologic disease
neurologic disease, diagnoses of
neurologic testing
neuromyotonia
neuronal degeneration
neuronopathy
neuropathology
neuropathy
neuropathy, diabetic
neuropathy, hereditary peripheral
next-generation sequencing
nusinersen
optic atrophy
pain, increased response
palliative care
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
Parkinson disease
Parkinson disease, dementia with
Parkinson disease, familial
Parkinson disease, rapid progression
Parkinson disease, young onset
Parkinsonism syndrome
Parkinsonism-dementia complex
paroxysmal neurologic deficits
patient information and support
peroneal muscle atrophy, causes of
peroxisomal disease
personality change
pleocytosis of cerebrospinal fluid
poison, mercury
poison, neurologic problems with
poliomyelitis
polyglucosan body
polyglucosan body disease
polymyositis
polyneuropathy
porphyria
post polio syndrome
preclinical
pregnancy, neurologic complications in
primary lateral sclerosis
prognosis
progressive neurologic disorder
progressive spinal muscular atrophy
pseudobulbar palsy
pseudohypertrophy
psychiatric problems in neurologic disorders
psychomotor retardation
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
radiculopathy
recombinant DNA
Refsum's disease
release phenomena
respirator
respiratory failure
review article
RFLPs
riluzole
risk factors
Roussy Levy syndrome
sarcoidosis
scoliosis
scoliosis, neurologic association with
screening
seizure
single photon emission computed tomography
skin, lesions in neurologic disorders
SMN1 gene
spastic ataxia
spasticity
speech disorder
speech, loss of
spinal cord
spinal cord degeneration
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spinocerebellar ataxia
stereotyped behavior
stiff man syndrome
superoxide dismutase
survival motor neuron gene
temporal lobe, atrophy
term infant
tongue, atrophy
tongue, fasciculations of
tongue, impaired movements of
tongue, weakness
torticollis
trauma
treatment of neurologic disorder
tremor
tremor, postural
tricresylphosphate
trinucleotide repeats
urea-cycle enzymopathies
urinary incontinence
vestibular function, tests of
walking, difficulty with
weakness
weakness, generalized
weakness, infant
weakness, progressive
weight loss
Werdnig-Hoffman disease
wheelchair
white matter disease
word-finding difficulty
X-linked bulbospinal neuronopathy
Showing articles 1000 to 1050 of 4485 << Previous Next >>

Tremor
JAMA 311:948-954, Elias, W.J. & Shah, B.B., 2014

Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
NEJM 370:911-920, Zhou, Q.,et al, 2014

Autism
Lancet 383:896-910, Lai, M.C.,et al, 2014

Relapsing-Remitting Tumefactive Demyelination
JAMA Neurol 71:366-367, Brandao, E.,et al, 2014

Daclizumab-Induced Adverse Events in Multiple Organ Systems in Multiple Sclerosis
Neurol 82:984-988, Oh, J.,et al, 2014

Summary of Evidence-Based Guideline: Complementary and Alternative Medicine in Multiple Sclerosis
Neurol 82:1083-1092, Yadav, V.,et al, 2014

Complementary and Alternative Medicine in Multiple Sclerosis
Neurol 82:e103-e104, Fox, R.J., 2014

Effect of high-dose Simvastatin on Brain Atrophy and Disability in Secondary Progressive Multiple Sclerosis (MS-STAT): A Randomised, Placebo-Controlled, Phase 2 Trial
Lancet 383:2213-2221, Chataway, J.,et al, 2014

Recommendations for the Management of Cerebral and Cerebellar Infarction with Swelling
Stroke 45:1222-1238, Wijdicks, E.F.M.,et al, 2014

Hemicraniectomy in Older Patients with Extensive Middle-Cerebral-Artery Stroke
NEJM 370:1091-1100,1159, Juttler, E.,et al, 2014

Everolimus Treatment of Refractory Epilepsy in Tuberous Sclerosis Complex
Ann Neurol 74:679-687, Krueger, D.A.,et al, 2013

Subacute Sclerosing Panencephalitis
www.MedLink.com, February, Auwaeter,P.G.&Johnson,R.T., 2013

Predicting Alzheimer Disease with �-Amyloid Imaging: Results from the Australian Imaging, Biomarkers, and Lifestyle Study of Ageing
Ann Neurol 74:905-913, Rowe, C.C.,et al, 2013

An Expanded Role for Neuroimaging in the Evaluation of Memory Impairment
AJNR 34:2075-2082, Desikan, R.S.,et al, 2013

Isolated Sphenoiditis
Neurol 81:e176, Safouris, A.,et al, 2013

Clinical Features of MS Associated with Leber Hereditary Optic Neuropathy mtDNA Mutations
Neurol 81:2073-2081, Pfeffer, G.,et al, 2013

Clinicopathologic Conference, Dissection of the left vertebral artery and cerebellar infarction
NEJM 369:1736-1748, Case 34-2013, 2013

Chediak-Higashi Syndrome: Pathognomonic Feature
Lancet 382:1514, Antunes, H.,et al, 2013

Tumefactive MS Lesions under Fingolimod
Neurol 81:1654-1658, Pilz, G.,et al, 2013

Extending the KCNQ2 encephalopathy Spectrum
Neurol 81:1697-1703, Weckhuysen, S.,et al, 2013

Longitudinally Extensive Transverse Myelitis with and Without Aquaporin 4 Antibodies
JAMA Neurol 70:1375-1381, Kitley, J.,et al, 2013

Head Drop in Huntington Disease: Insights into the Pathophysiology
Neurol 81:769-770, Morgante, F.,et al, 2013

Tolosa-Hunt Syndrome - a Rare Cause of Headache and Ophthalmoplegia
Lancet 382:912, Zurawski, J. & Akhondi, H., 2013

Interdependence and Contributions of Sun Exposure and Vitamin D to MRI Measures in Multiple Sclerosis
JNNP 84:1075-1081, 1066, Zivadinov, R.,et al, 2013

MRI-Identified Pathology in Adults with New-Onset Seizures
Neurol 81:920-927, Hakami, T.,et al, 2013

Revised Diagnostic Criteria for the Pseudotumor Cerebri Syndrome in Adults and Children
Neurol 81:1159-1165, Friendman, D.I.,et al, 2013

Painful Ophthalmoplegia Following Dental Procedure
Neuroophthalmol 37:165-168, Simsek, I.,et al, 2013

Mystery Case: A Young Boy with Myoclonic Jerks
Neurol 81:e130-e134, Musleh, C.,et al, 2013

Cerebral Venous Thrombosis after High Dose Steroid in Multiple Sclerosis: A Case Report
Hippokratia 17:88-90, Gazioglu, S.,et al, 2013

Spinal Cord Lesions in Patients with Clinically Isolated Syndrome
Neurol 80:69-75, Sombekke, M.,et al, 2013

Functional Impairment in Progressive Supranuclear Palsy
Neurol 80:380-384, Duff, K.,et al, 2013

Clinicopathologic Conference, Cholesteatoma & Cholesterol Granuloma with Chronic Otitis Media, with Dural SinusThrombosis
NEJM 368:267-277, Case 2-2013, 2013

Clinical Course of Idiopathic Intracranial Hypertension with Transverse Sinus Stenosis
Neurol 80:289-295, Riggeal, B.,et al, 2013

Location of Brain Lesions Predicts Conversion of Clinically Isolated Syndromes to Multiple Sclerosis
Neurol 80:234-241, Giorgio, A.,et al, 2013

Everolimus Long-Term Safety and Efficacy in Subependymal Giant Cell Astrocytoma
Neurol 80:574-580, Krueger, D.,et al, 2013

Tumor Necrosis Factor-Alpha Inhibitors: An Overview of Adverse Effects
UpToDate January, Stone, J.H., 2013

Interferon beta for Secondary Progressive Multiple Sclerosis: A Systematic Review
JNNP 84:420-426, La Mantia, L.,et al, 2013

Disability in Multiple Sclerosis
Neurol 80:1018-1024, Kister, I.,et al, 2013

Peripheral Neuropathy - Lead Astray?
LANCET 381:1156, Pickrell, W.,et al, 2013

Daclizumab High-Yield Process in Relapsing-Remitting Multiple Sclerosis (SELECT): A Randomised, Double-Blind, Placebo-Controlled Trial
Lancet 381:190-194, Gold, R.,et al, 2013

Varicella-Zoster Virus Acute Myelitis in a Patient with MS Treated with Natalizumab
Neurol 80:1812-1813, Yeung, J.,et al, 2013

Longitudinally Extensive Transverse Myelitis in Neuro-Beh�et Disease
Neurol 80:e189-e190, Graham, D.,et al, 2013

Reversible Ondines Curse in a Case of Lateral Medullary Infarction
Neurol 80:e13-e16, Mendoza, M. & Latorre, J., 2013

The Thalamus and Multiple Sclerosis
Neurol 80:210-219, Minagar, A.,et al, 2013

Aquaporin-4 Antibody-Negative Neuromyelitis Optica
Neurol 80:2194-2200,2176, Maringer, R.,et al, 2013

Aquaporin-4 Antibody-Positive Cases Beyond Current Diagnosis Criteria for NMO Spectrum Disorders
Neurol 80:2210-2216, Sato, D.,et al, 2013

Daclizumab High-Yield Process in Relapsing-Remitting Multiple Sclerosis (SELECT): A Randomised, Double-Blind, Placebo-Controlled Trial
Lancet 381:2167-2175, Gold, R.,et al, 2013

Clinicopathologic Conference, Blind and Confused, Neuromyelitis Optica Spectrum Disorder
JAMA Neurol 70:932-936, Sharma, V.,et al, 2013

Extensive Vasogenic Edema of Anti-Aquaporin-4 Antibody-Related Brain Lesions
Mult Scler 15:1113-1117, Matsushita, T.,et al, 2013

Brain Abnormalities as an Initial Manifestation of Neuromyelitis Optica Spectrum Disorder
MSJ 17:1107-1112, Kim, W.,et al, 2013



Showing articles 1000 to 1050 of 4485 << Previous Next >>